General Info

TAG offers expertise in global GCP and GLP Quality Assurance and Clinical Research. TAG principals, have over 25 years of global experience in the drug and device industry working for sponsor and CRO organizations in positions of QA, Training and Development, Standard Operating Procedures, and Clinical Research. TAG is also networked with other consultants who assist with larger scale projects or niche areas, such as Part 11 validation work or GMP process validation. CV and references are available upon request.